Structure of murine angiogenin: features of the substrate- and cell-binding regions and prospects for inhibitor-binding studies.

ABSTRACT: Angiogenin is an unusual member of the pancreatic ribonuclease superfamily that induces blood-vessel formation and is a promising anticancer target. The three-dimensional structure of murine angiogenin (mAng) has been determined by X-ray crystallography. Two structures are presented: one is a complex with sulfate ions (1.5 Angstroms resolution) and the other a complex with phosphate ions (1.6 Angstroms resolution). Residues forming the putative B(1), P(1) and B(2) subsites occupy positions similar to their hAng counterparts and are likely to play similar roles. The anions occupy the P(1) subsite, sulfate binding conventionally and phosphate adopting two orientations, one of which is novel. The B(1) subsite is obstructed by Glu116 and Phe119, with the latter assuming a less invasive positio

SUBMITTER: Holloway DE 

PROVIDER: S-EPMC1780170 | biostudies-literature | 2005 Dec

REPOSITORIES: biostudies-literature